FDA Inspection 719451 — Lockheed Martin Gyrocam Systems, Inc.
The FDA completed an inspection of Lockheed Martin Gyrocam Systems, Inc. on April 8, 2011 in Sarasota, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- April 8, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Sarasota, FL (United States)